Evidence map›Paper›PMID 23457214›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2013

Differential regulation of proteasome functionality in reproductive vs. somatic tissues of Drosophila during aging or oxidative stress.

Eleni N Tsakiri, Gerasimos P Sykiotis, Issidora S Papassideri, Vassilis G Gorgoulis, Dirk Bohmann, Ioannis P Trougakos

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03543579 (An Observational Study of Cardiovascular Complications of Carfilzomib Treatment in Clinical Practice), which is not on this map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
3.6field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03543579 unknown statusnot on this mapstarted 2017, after this paper: background citation

An Observational Study of Cardiovascular Complications of Carfilzomib Treatment in Clinical Practice

TypeobservationalSponsorUniversity of AthensRan2017 to 2021Enrolled46ConditionsMultiple Myeloma
3 · Its place in the literature

Who cites it

56 citing papers in PubMed, 92 citations in OpenAlex.

  1. Trial
  2. Proteostasis and ageing dissidence.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2026
    Review
  3. The Ancestral KEAP1-NRF Pathway in AmphioxusInternational journal of molecular sciences · 2025
    Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Molecular basis of reproductive senescence: insights from model organisms.Journal of assisted reproduction and genetics · 2021
    Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. The proteostasis network and its decline in ageing.Nature reviews. Molecular cell biology · 2019
    Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 2 countries.

Eleni N TsakiriDepartment of Cell Biology and Biophysics, Faculty of Biology, University of Athens, Panepistimiopolis, Athens, Greece.
Gerasimos P Sykiotis
Issidora S Papassideri
Vassilis G Gorgoulis
Dirk Bohmann
Ioannis P Trougakos
National and Kapodistrian University of Athens · GRAthens State University · USUniversity of Patras · GRUniversity of Rochester Medical Center · US

Funding

Nrf2 as a regulator of health span and agingR01AG039753 · NIA · UNIVERSITY OF ROCHESTER · PI BOHMANN, DIRK · 2011 to 2015
$1.6M
NIA NIH HHS R01 AG039753
6 · The paper itself

Abstract

Proteasome is central to proteostasis maintenance, as it degrades both normal and damaged proteins. Herein, we undertook a detailed analysis of proteasome regulation in the in vivo setting of Drosophila melanogaster. We report that a major hallmark of somatic tissues of aging flies is the gradual accumulation of ubiquitinated and carbonylated proteins; these effects correlated with a ~50% reduction of proteasome expression and catalytic activities. In contrast, gonads of aging flies were relatively free of proteome oxidative damage and maintained substantial proteasome expression levels and highly active proteasomes. Moreover, gonads of young flies were found to possess more abundant and more active proteasomes than somatic tissues. Exposure of flies to oxidants induced higher proteasome activities specifically in the gonads, which were, independently of age, more resistant than soma to oxidative challenge and, as analyses in reporter transgenic flies showed, retained functional antioxidant responses. Finally, inducible Nrf2 activation in transgenic flies promoted youthful proteasome expression levels in the aged soma, suggesting that age-dependent Nrf2 dysfunction is causative of decreasing somatic proteasome expression during aging. The higher investment in proteostasis maintenance in the gonads plausibly facilitates proteome stability across generations; it also provides evidence in support of the trade-off theories of aging.

Indexed as

AgingAnimalsAnimals, Genetically ModifiedAntioxidant Response ElementsDrosophila melanogasterDrosophila ProteinsFemaleGenes, InsectIntracellular Signaling Peptides and ProteinsKelch-Like ECH-Associated Protein 1MaleNF-E2-Related Factor 2OvaryProteasome Endopeptidase ComplexTestisTissue DistributionDrosophila ProteinsIntracellular Signaling Peptides and ProteinsKeap1 protein, DrosophilaKelch-Like ECH-Associated Protein 1NF-E2-Related Factor 2Proteasome Endopeptidase Complexantioxidant response elementsgonadsKeap1Nrf2

Identifiers

PMID23457214
PMCPMC4050428
OpenAlexW2092285861

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.